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rs4676049

From SNPedia

Orientationplus
Stabilizedplus
Make rs4676049(C;C)
Make rs4676049(C;T)
Make rs4676049(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position109018801
is asnp
is mentioned by
dbSNPrs4676049
ebirs4676049
HLIrs4676049
Exacrs4676049
Varsomers4676049
Maprs4676049
PheGenIrs4676049
hapmaprs4676049
1000 genomesrs4676049
hgdprs4676049
ensemblrs4676049
gopubmedrs4676049
geneviewrs4676049
scholarrs4676049
googlers4676049
pharmgkbrs4676049
gwascentralrs4676049
openSNPrs4676049
23andMers4676049
23andMe allrs4676049
SNP Nexus

SNPshotrs4676049
SNPdbers4676049
MSV3drs4676049
GWAS Ctlgrs4676049
GMAF0.1396
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20885792OA-icon.png]
Trait
Title Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities
Risk Allele A
P-val 4E-8
Odds Ratio 1.76 [1.44-2.15]